{{Rsnum
|rsid=467650
|Chromosome=5
|position=98633749
|Orientation=plus
|GMAF=0.3457
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 9.7 | 42.5 | 47.8
| HCB | 0.7 | 20.4 | 78.8
| JPT | 0.9 | 17.1 | 82.0
| YRI | 48.9 | 43.3 | 7.8
| ASW | 42.1 | 45.6 | 12.3
| CHB | 0.7 | 20.4 | 78.8
| CHD | 0.9 | 18.5 | 80.6
| GIH | 5.9 | 34.7 | 59.4
| LWK | 43.9 | 46.7 | 9.3
| MEX | 12.3 | 31.6 | 56.1
| MKK | 41.0 | 45.5 | 13.5
| TSI | 7.8 | 50.0 | 42.2
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23509962
  |Trait=Venous thromboembolism (gene x gene interaction)
  |Title=A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosis.
  |RiskAllele=
  |Pval=1E-8
  |OR=1.49
  |ORtxt=[NR]
  |OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}